A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706015



Internal ID15442667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:96975341..96981627hg38UCSC Ensembl
Innerchr1:97440897..97447183hg19UCSC Ensembl
Innerchr1:97213485..97219771hg18UCSC Ensembl
Innerchr1:97152918..97159204hg17UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386287
hg196287
hg186287
hg176287
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522619
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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